ASTM-F1635 › Historical Revision Information
Standard Test Method for In Vitro Degradation Testing of Poly (L-lactic Acid) Resin and Fabricated Form for Surgical Implants
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Standard Test Method for in vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants
Scope
1.1 This test method covers poly(L-lactic acid) resin intended for use in surgical implants.
1.2 The requirements of this test method apply to poly(Llactic acid) in various forms:
1.2.1 Virgin polymer, or
1.2.2 Any form fabricated from virgin polymer such as a semi-finished component of a finished product, a finished product, which may include packaged and sterilized implants, or a specially fabricated test specimen.
Keywords
bioabsorbable; degradation; in vitro; PLA, poly(L-lactic acid); polymer; surgical implants; ICS Number Code 11.040.40 (Implants for surgery, prothetics and orthotics)
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13.01 (Medical and Surgical Materials and Devices)
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Document Number
ASTM-F1635-95(2000)
Revision Level
1995 R00 EDITION
Status
Superseded
Modification Type
Reapproval
Publication Date
Nov. 10, 1995
Document Type
Test Method
Page Count
4 pages
Committee Number
F04.15